Evidence map›Paper›PMID 40813446›Full record

SynthesisScientific reports2025

Impact of tumor necrosis factor-alpha gene variant in pediatric nephrotic syndrome: a meta-analysis.

Yogalakshmi Venkatachalapathy, Praveenkumar Kochuthakidiyel Suresh, Thendral Hepsibha Balraj, Vettriselvi Venkatesan, Sangeetha Geminiganesan, Indira Bhagam, C D Mohana Priya

Erratum issuedAbstract readMeta-Analysis
In one paragraph

Synthesis in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Yogalakshmi VenkatachalapathyDepartment of Human Genetics, Sri Ramachandra Institute of Higher Education and Research, Chennai, India.ORCID http://orcid.org/0000-0002-3795-5930
Praveenkumar Kochuthakidiyel SureshDepartment of Human Genetics, Sri Ramachandra Institute of Higher Education and Research, Chennai, India.ORCID http://orcid.org/0009-0001-2824-1469
Thendral Hepsibha BalrajDepartment of Biochemistry, Ethiraj College for Women, Chennai, India.ORCID http://orcid.org/0000-0002-5041-3925
Vettriselvi VenkatesanDepartment of Human Genetics, Sri Ramachandra Institute of Higher Education and Research, Chennai, India.ORCID http://orcid.org/0000-0003-2827-8680
Sangeetha GeminiganesanKauvery Hospital, Chennai, India.ORCID http://orcid.org/0000-0003-0734-1126
Indira BhagamSri Ramachandra Institute of Higher Education and Research, Chennai, India.
C D Mohana PriyaDepartment of Human Genetics, Sri Ramachandra Institute of Higher Education and Research, Chennai, India. mohanapriya@sriramachandra.edu.in.ORCID http://orcid.org/0000-0001-6760-785X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aims to explore the risk associated with the Tumour Necrosis Factor-Alpha (TNFα)-308 G/A (rs1800629) gene polymorphism in relation to Childhood Nephrotic Syndrome (NS). The primary goal of the meta-analysis was to investigate the relationship between Nephrotic Syndrome and the TNFα 308 G/A [rs1800629] polymorphism of the cytokine gene. We conducted a systematic search across electronic databases like PubMed and Google Scholar to collect data from five distinct case-control studies focused on the TNFα 308 G/A gene variant, covering the period from 2010 to 2022. By aggregating allele and genotype frequencies from these studies, we computed the 95% confidence interval of odds ratio [OR] to assess the strength of the association. To evaluate heterogeneity and potential publication bias in the selected studies, Stats Direct software was employed. The sample size encompassed 1,560 individuals, including 628 cases and 932 controls from five separate case-control studies. The TNFα allele-A displayed significant heterogeneity [I²=80%, 95% CI] when compared to the G allele, and a statistically significant pooled OR of 2.32 [P = 0.0056*] was observed. In the overall analysis, no significance association was found in the dominant model [P = 0.068], but a significant association was detected in the recessive model [P = 0.0096*]. Consistent findings were observed in the co-dominant model, where both AA vs. GG [P = 0.0075*] and GA vs. GG [P = 0.0219*] showed significant associations. These results suggest a potential increase in the risk of the disease associated with the polymorphism of TNFα 308 G/A. The small number of studies, high heterogeneity (I² = 80%), and limited ethnic diversity may affect the robustness and generalizability of findings. Additionally, language bias and lack of confounder adjustment limit interpretability. The TNFα 308 G/A polymorphism was identified as being associated with the risk of developing childhood NS.Registration: Registered in PROSPERO with ID: CRD420251083425.

Indexed as

Genetic Predisposition to DiseaseNephrotic SyndromePolymorphism, Single NucleotideTumor Necrosis Factor-alphaAllelesCase-Control StudiesChildGene FrequencyGenotypeHumansTumor Necrosis Factor-alphaChildhood nephrotic syndromeGenetic variantMeta-analysisPediatricsTNF-α polymorphism

Identifiers

PMID40813446
PMCPMC12354666

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.